Lafora disease
type of rare, inherited, severe, progressive myoclonic epilepsy
Press Enter · cited answer in seconds
0 sources
Lafora disease
Summary
Lafora disease is a rare disease[1]. It draws 76 Wikipedia views per month (rare_disease category, ranking #188 of 627).[2]
Key Facts
- Lafora disease's instance of is recorded as rare disease[3].
- Lafora disease's instance of is recorded as class of disease[4].
- Gonzalo Rodríguez Lafora is named after Lafora disease[5].
- Lafora disease's subclass of is recorded as neurodegeneration[6].
- Lafora disease's subclass of is recorded as progressive myoclonus epilepsy[7].
- Lafora disease's subclass of is recorded as nervous system heredodegenerative disease[8].
- Lafora disease's subclass of is recorded as progressive epilepsy and/or ataxia with myoclonus as a major feature[9].
- Lafora disease's subclass of is recorded as autosomal recessive disease[10].
- Lafora disease's MeSH descriptor ID is recorded as D020192[11].
- Lafora disease's OMIM ID is recorded as 254780[12].
- Lafora disease's ICD-9 ID is recorded as 345.1[13].
- Lafora disease's ICD-10 ID is recorded as G40.3[14].
- Lafora disease's DiseasesDB is recorded as 30834[15].
- Lafora disease's Freebase ID is recorded as /m/04jv0[16].
- Lafora disease's KEGG ID is recorded as H01994[17].
- Lafora disease's ICPC 2 ID is recorded as N88[18].
- Lafora disease's GeneReviews ID is recorded as NBK1389[19].
- Lafora disease's MeSH tree code is recorded as C10.574.500.529[20].
- Lafora disease's MeSH tree code is recorded as C16.320.400.480[21].
- Lafora disease's MeSH tree code is recorded as C10.228.140.490.493.063.650.500[22].
- Lafora disease's MeSH tree code is recorded as C10.228.140.490.375.130.650.500[23].
- Lafora disease's Disease Ontology ID is recorded as DOID:3534[24].
- Lafora disease's symptoms and signs is recorded as hallucination[25].
- Lafora disease's Orphanet ID is recorded as 501[26].
- Lafora disease's NCI Thesaurus ID is recorded as C84804[27].
Why It Matters
Lafora disease draws 76 Wikipedia views per month (rare_disease category, ranking #188 of 627).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] It is known by 17 alternative names across languages and contexts.[29]